Investigating neurodevelopmental defects in metabolic disease MELAS using 3D organoid model
Mitochondrial encaphalomyopathy, lactic acidosis, and stroke like episodes (MELAS) syndrome is a disorder caused by mutation in mitochondria DNA. MELAS syndrome is characterized by a myriad of multi-organs symptoms such as seizures, vomiting, muscle weakness and diabetes. One of the most causal gene...
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| Format: | Final Year Project |
| Language: | English |
| Published: |
2018
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| Online Access: | http://hdl.handle.net/10356/74682 |
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| Institution: | Nanyang Technological University |
| Language: | English |